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About This Item
Empirical Formula (Hill Notation):
C8H6ClN
CAS Number:
Molecular Weight:
151.59
Beilstein:
112345
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
form
solid
mp
87-90 °C (lit.)
solubility
ethanol: 50 mg/mL, clear, colorless to faintly yellow
SMILES string
Clc1ccc2cc[nH]c2c1
InChI
1S/C8H6ClN/c9-7-2-1-6-3-4-10-8(6)5-7/h1-5,10H
InChI key
YTYIMDRWPTUAHP-UHFFFAOYSA-N
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General description
6-Chloroindole, when added to Claviceps purpurea, produced the corresponding substituted L-tryptophan.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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D S Fukuda et al.
Applied microbiology, 21(5), 841-843 (1971-05-01)
Claviceps purpurea has been shown to produce extracellular l-tryptophan from indole in stirred fermentors. The substrate specificity of this conversion was investigated by using substituted indoles, anthranilic acid, and 4-chloro-anthranilic acid. Addition of 2-, 4-, 5-, 6-, and 7-methyl indole
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Multi-drug resistant Acinetobacter baumannii is well-known for its rapid acclimatization in hospital environments. The ability of the bacterium to endure desiccation and starvation on dry surfaces for up to a month results in outbreaks of health care-associated infections. Previously, indole
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Because of the pivotal role of cyclooxygenase (COX) in the inflammatory processes, non-steroidal anti-inflammatory drugs (NSAIDs) that suppress COX activities have been used clinically for the treatment of inflammatory diseases/syndromes; however, traditional NSAIDs exhibit serious side-effects such as gastrointestinal damage
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